TY - JOUR
T1 - Long-term cancer-specific outcomes of TaG1 urothelial carcinoma of the bladder
AU - Rieken, Malte
AU - Xylinas, Evanguelos
AU - Kluth, Luis
AU - Crivelli, Joseph J.
AU - Chrystal, James
AU - Faison, Talia
AU - Lotan, Yair
AU - Karakiewicz, Pierre I.
AU - Holmäng, Sten
AU - Babjuk, Marek
AU - Fajkovic, Harun
AU - Seitz, Christian
AU - Klatte, Tobias
AU - Pycha, Armin
AU - Bachmann, Alexander
AU - Scherr, Douglas S.
AU - Shariat, Shahrokh F.
N1 - Funding Information:
Financial disclosures: Shahrokh F. Shariat certifies that all conflicts of interest, including specific financial interests and relationships and affiliations relevant to the subject matter or materials discussed in the manuscript (eg, employment/affiliation, grants or funding, consultancies, honoraria, stock ownership or options, expert testimony, royalties, or patents filed, received, or pending), are the following: Malte Rieken has received grant support from the Swiss National Science Foundation. Alexander Bachmann has been a consultant for American Medical Systems, Orion Pharma, Schering, Olympus, and Caris Life Sciences. Shahrokh F. Shariat has been on the advisory board for Ferring Pharmaceutics.
PY - 2014/1
Y1 - 2014/1
N2 - Background Few studies have investigated the natural history of TaG1 urothelial carcinoma of the bladder (UCB). Objective To assess the long-term outcomes of patients with TaG1 UCB and the impact of immediate postoperative instillation of chemotherapy (IPIC). Design, setting, and participants A retrospective analysis of 1447 patients with TaG1 UCB treated between 1996 and 2007 at eight centers. Median follow-up was 67.2 mo (interquartile range: 67.9). Patients were stratified into three European Association of Urology (EAU) guidelines risk categories; high-risk patients (n = 11) were excluded. Intervention Transurethral resection of the bladder with or without IPIC. Outcome measurements and statistical analysis Univariable and multivariable Cox regression models addressed factors associated with disease recurrence, disease progression, death of disease, and any-cause death. Results and limitations Of the 1436 patients, 601 (41.9%) and 835 (58.1%) were assigned to low- and intermediate-risk categories, respectively. The actuarial estimate of 5-yr recurrence-free survival was 56% (standard error: ±1). Advancing age (p = 0.04), tumor >3 cm (p = 0.001), multiple tumors (p < 0.001), and recurrent tumors (p < 0.001) were independently associated with increased risk of disease recurrence, whereas IPIC was associated with decreased risk (p = 0.001). The actuarial estimate of 5-yr progression-free survival was 95% ± 1. Advancing age (p < 0.001) and multiple tumors (p = 0.01) were independent risk factors for disease progression. Five-year cancer-specific survival was 98% ± 1. Advancing age (p = 0.001) and previous recurrence (p = 0.04) were associated with increased risk, whereas female gender (p = 0.02) was associated with decreased risk of cancer-specific mortality. Compared with low-risk patients, intermediate-risk patients were at significantly higher risk of disease recurrence, disease progression, and cancer-specific mortality (all p < 0.01). Limitations include the retrospective design of the study and the lack of a central pathology review. Conclusions TaG1 UCB patients experience heterogeneous risks of disease recurrence. We validated the EAU guidelines risk stratification in TaG1 UCB patients. IPIC was associated with a reduced risk of disease recurrence in patients with low- and intermediate-risk TaG1 UCB.
AB - Background Few studies have investigated the natural history of TaG1 urothelial carcinoma of the bladder (UCB). Objective To assess the long-term outcomes of patients with TaG1 UCB and the impact of immediate postoperative instillation of chemotherapy (IPIC). Design, setting, and participants A retrospective analysis of 1447 patients with TaG1 UCB treated between 1996 and 2007 at eight centers. Median follow-up was 67.2 mo (interquartile range: 67.9). Patients were stratified into three European Association of Urology (EAU) guidelines risk categories; high-risk patients (n = 11) were excluded. Intervention Transurethral resection of the bladder with or without IPIC. Outcome measurements and statistical analysis Univariable and multivariable Cox regression models addressed factors associated with disease recurrence, disease progression, death of disease, and any-cause death. Results and limitations Of the 1436 patients, 601 (41.9%) and 835 (58.1%) were assigned to low- and intermediate-risk categories, respectively. The actuarial estimate of 5-yr recurrence-free survival was 56% (standard error: ±1). Advancing age (p = 0.04), tumor >3 cm (p = 0.001), multiple tumors (p < 0.001), and recurrent tumors (p < 0.001) were independently associated with increased risk of disease recurrence, whereas IPIC was associated with decreased risk (p = 0.001). The actuarial estimate of 5-yr progression-free survival was 95% ± 1. Advancing age (p < 0.001) and multiple tumors (p = 0.01) were independent risk factors for disease progression. Five-year cancer-specific survival was 98% ± 1. Advancing age (p = 0.001) and previous recurrence (p = 0.04) were associated with increased risk, whereas female gender (p = 0.02) was associated with decreased risk of cancer-specific mortality. Compared with low-risk patients, intermediate-risk patients were at significantly higher risk of disease recurrence, disease progression, and cancer-specific mortality (all p < 0.01). Limitations include the retrospective design of the study and the lack of a central pathology review. Conclusions TaG1 UCB patients experience heterogeneous risks of disease recurrence. We validated the EAU guidelines risk stratification in TaG1 UCB patients. IPIC was associated with a reduced risk of disease recurrence in patients with low- and intermediate-risk TaG1 UCB.
KW - Immediate postoperative intravesical chemotherapy
KW - Outcome assessment
KW - TaG1 urothelial carcinoma of the bladder
KW - Transurethral resection
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U2 - 10.1016/j.eururo.2013.08.034
DO - 10.1016/j.eururo.2013.08.034
M3 - Article
C2 - 23998688
AN - SCOPUS:84888825186
SN - 0302-2838
VL - 65
SP - 201
EP - 209
JO - European Urology
JF - European Urology
IS - 1
ER -